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Monkey C3b (Complement Fragment 3b) ELISA Kit

SKU:
AEFI00459
Product Type:
ELISA Kit
Size:
96 Assays
Sensitivity:
0.188ng/ml
Range:
0.313-20ng/ml
ELISA Type:
Sandwich
Reactivity:
Monkey
  • Monkey C3b (Complement Fragment 3b) ELISA Kit
  • Monkey C3b (Complement Fragment 3b) ELISA Kit
€649
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Description

Monkey C3b (Complement Fragment 3b) ELISA Kit

The Monkey C3b Complement Fragment 3b ELISA Kit is specifically developed for the precise measurement of C3b complement fragment 3b levels in monkey serum, plasma, and cell culture supernatants. This kit boasts exceptional sensitivity and specificity, ensuring accurate and consistent results for a variety of research purposes.C3b complement fragment 3b is a critical component of the complement system, playing a key role in immune responses and inflammation.

Dysregulation of this fragment has been linked to various diseases and disorders, emphasizing its importance as a biomarker for studying these conditions and exploring potential treatment options.With its advanced technology and reliable performance, the Monkey C3b Complement Fragment 3b ELISA Kit is an invaluable tool for researchers seeking to further their understanding of immune responses and inflammatory processes in monkeys.

Product Name:Monkey C3b (Complement Fragment 3b) ELISA Kit
Product Code:AEFI00459
Size:96T
Alias:C3b, Complement Fragment 3b
Detection method:Sandwich ELISA, Double Antibody
Application:C3b ELISA Kit allows for the in vitro quantitative determination of C3b concentrations in serum, plasma, tissue homogenates and other biological fluids.
Sensitivity:< 0.188ng/ml
Range:0.313-20ng/ml
Storage:2-8°C for 6 months
Note:For Research Use Only
Recovery: Matrices listed below were spiked with certain level of C3b and the recovery rates were calculated by comparing the measured value to the expected amount of C3b in samples.
MatrixRecovery range(%)Average(%)
serum(n=5)88-10595
EDTA plasma(n=5)88-9994
heparin plasma(n=5)89-10598
Linearity: The linearity of the kit was assayed by testing samples spiked with appropriate concentration of C3b and their serial dilutions. The results were demonstrated by the percentage of calculated concentration to the expected.
Sample1:21:41:8
serum(n=5)87-102%86-105%86-104%
EDTA plasma(n=5)84-96%82-100%82-99%
heparin plasma(n=5)87-98%80-99%84-96%
CV(%): Intra-Assay: CV<8%
Inter-Assay: CV<10%

When carrying out an ELISA assay it is important to prepare your samples in order to achieve the best possible results. Below we have a list of procedures for the preparation of samples for different sample types.

Sample TypeProtocol
Serum If using serum separator tubes, allow samples to clot for 30 minutes at room temperature. Centrifuge for 10 minutes at 1,000x g. Collect the serum fraction and assay promptly or aliquot and store the samples at -80°C. Avoid multiple freeze-thaw cycles.

If serum separator tubes are not being used, allow samples to clot overnight at 2-8°C. Centrifuge for 10 minutes at 1,000x g. Remove serum and assay promptly or aliquot and store the samples at -80°C. Avoid multiple freeze-thaw cycles.

PlasmaCollect plasma using EDTA or heparin as an anticoagulant. Centrifuge samples at 4°C for 15 mins at 1000 × g within 30 mins of collection. Collect the plasma fraction and assay promptly or aliquot and store the samples at -80°C. Avoid multiple freeze-thaw cycles. Note: Over haemolysed samples are not suitable for use with this kit.
Urine & Cerebrospinal FluidCollect the urine (mid-stream) in a sterile container, centrifuge for 20 mins at 2000-3000 rpm. Remove supernatant and assay immediately. If any precipitation is detected, repeat the centrifugation step. A similar protocol can be used for cerebrospinal fluid.
Cell culture supernatantCollect the cell culture media by pipette, followed by centrifugation at 4°C for 20 mins at 1500 rpm. Collect the clear supernatant and assay immediately.
Cell lysatesSolubilize cells in lysis buffer and allow to sit on ice for 30 minutes. Centrifuge tubes at 14,000 x g for 5 minutes to remove insoluble material. Aliquot the supernatant into a new tube and discard the remaining whole cell extract. Quantify total protein concentration using a total protein assay. Assay immediately or aliquot and store at ≤ -20 °C.
Tissue homogenatesThe preparation of tissue homogenates will vary depending upon tissue type. Rinse tissue with 1X PBS to remove excess blood & homogenize in 20ml of 1X PBS (including protease inhibitors) and store overnight at ≤ -20°C. Two freeze-thaw cycles are required to break the cell membranes. To further disrupt the cell membranes you can sonicate the samples. Centrifuge homogenates for 5 mins at 5000xg. Remove the supernatant and assay immediately or aliquot and store at -20°C or -80°C.
Tissue lysatesRinse tissue with PBS, cut into 1-2 mm pieces, and homogenize with a tissue homogenizer in PBS. Add an equal volume of RIPA buffer containing protease inhibitors and lyse tissues at room temperature for 30 minutes with gentle agitation. Centrifuge to remove debris. Quantify total protein concentration using a total protein assay. Assay immediately or aliquot and store at ≤ -20 °C.
Breast MilkCollect milk samples and centrifuge at 10,000 x g for 60 min at 4°C. Aliquot the supernatant and assay. For long term use, store samples at -80°C. Minimize freeze/thaw cycles.

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